Expression of full-length Cochlin p63s is inner ear specific

Auris Nasus Larynx - Tập 32 - Trang 219-223 - 2005
Lishu Li1, Tetsuo Ikezono1, Atsushi Watanabe2, Susumu Shindo1, Ruby Pawankar1, Toshiaki Yagi1
1Department of Otorhinolaryngology, Nippon Medical School, 1-1-5, Sendagi Bunkyo-ku, Tokyo 113-8603, Japan
2Department of Biochemistry and Molecular Biology, Nippon Medical School, Tokyo

Tài liệu tham khảo

Verhagen, 2000, Familial progressive vestibulocochlear dysfunction caused by a COCH mutation (DFNA9), Arch Neurol, 57, 1045, 10.1001/archneur.57.7.1045

Verstreken, 2001, Hereditary otovestibular dysfunction and Meniere's disease in a large Belgian family is caused by a missense mutation in the COCH gene, Otol Neurotol, 22, 874, 10.1097/00129492-200111000-00028

de Kok, 1999, A Pro51Ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defects, Hum Mol Genet, 8, 361, 10.1093/hmg/8.2.361

Robertson, 1998, Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction, Nat Genet, 20, 299, 10.1038/3118

Manolis, 1996, A gene for non-syndromic autosomal dominant progressive postlingual sensorineural hearing loss maps to chromosome 14q12–13, Hum Mol Genet, 5, 1047, 10.1093/hmg/5.7.1047

Usami, 2003, Mutations in the COCH gene are a frequent cause of autosomal dominant progressive cochleo-vestibular dysfunction, but not of Meniere's disease, Eur J Hum Genet, 11, 744, 10.1038/sj.ejhg.5201043

Ikezono, 2001, Identification of the protein product of the COCH gene-hereditary deafness gene-as the major component of inner ear protein, Biochim Biophys Acta, 1535, 258, 10.1016/S0925-4439(00)00101-0

Solares, 2004, Murine autoimmune hearing loss mediated by CD4+ T cells specific for inner ear peptides, J Clin Invest, 113, 1210, 10.1172/JCI200418195

Zhang, 1989, Sequence and tissue distribution of a second protein of hepatic gap junctions, Cx26, as deduced from its cDNA, J Cell Biol, 109, 3391, 10.1083/jcb.109.6.3391

Abe, 2003, Identification of CRYM as a candidate responsible for nonsyndromic deafness, through cDNA microarray analysis of human cochlear and vestibular tissue, Am J Hum Genet, 72, 73, 10.1086/345398

Robertson, 1997, Mapping and characterization of a novel cochlear gene in human and in mouse: a positional candidate gene for a deafness disorder, DFNA9, Genomics, 46, 345, 10.1006/geno.1997.5067

Rodriguez, 2004, Cochlin a secreted von Willebrand factor type a domain-containing factor, is regulated by leukemia inhibitory factor in the uterus at the time of embryo implantation, Endocrinology, 145, 1410, 10.1210/en.2003-1361

Trexler, 2000, The LCCL module, Eur J Biochem, 267, 5751, 10.1046/j.1432-1327.2000.01641.x